Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.890 1.000 12 2007 2019
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.880 1.000 10 2007 2018
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 10 2011 2018
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1168443
Disease: Pseudocholinesterase Measurement
Pseudocholinesterase Measurement
0.700 1.000 1 2011 2011
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0017638
Disease: Glioma
Glioma
0.700 1.000 1 2011 2011
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2013 2013
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.030 1.000 3 2013 2014
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.030 1.000 3 2013 2014
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2014 2018
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.020 1.000 2 2013 2014
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.020 1.000 2 2013 2016
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.010 1.000 1 2018 2018
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0018799
Disease: Heart Diseases
Heart Diseases
0.010 1.000 1 2017 2017
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2013 2013
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0002962
Disease: Angina Pectoris
Angina Pectoris
0.010 1.000 1 2015 2015
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases
0.010 1.000 1 2013 2013
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2017 2017
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0007282
Disease: Carotid Stenosis
Carotid Stenosis
0.010 1.000 1 2019 2019
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2013 2013
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2018 2018
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2013 2013
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0007786
Disease: Brain Ischemia
Brain Ischemia
0.010 1.000 1 2019 2019